A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14370006



Internal ID22206289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24607496..24632197hg38UCSC Ensembl
chr14:25076702..25101403hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3824702
hg1924702
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220043
Supporting Variants
SamplesHG00732
Known GenesGZMB, GZMH
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14370006
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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